{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Waukesha",
      "address_1": "3000 N Grandview Blvd",
      "reason_for_recall": "An issue was identified with the mAs accuracy check performed on the system that could result in inaccuracies in the 10% to 20% range for exposure times longer than 15 msec.",
      "address_2": "",
      "product_quantity": "6 units in US",
      "code_info": "OptimaXR220amx  PN 5555000-5, PN5555000-6",
      "center_classification_date": "20150427",
      "distribution_pattern": "US Distribution to the states of: AZ, FL, GA, MO and WI.",
      "state": "WI",
      "product_description": "GE Healthcare Automatic Mobile X-Ray (AMX) Series:  Optima XR220 amx",
      "report_date": "20150506",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "GE Healthcare",
      "recall_number": "Z-1407-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "70924",
      "termination_date": "20150429",
      "more_code_info": "",
      "recall_initiation_date": "20141219",
      "postal_code": "53188-1615",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}